Expert In Drug Product Formulation And Processing For Synthetic Molecule Parenterals (cmc Advisor)

Roche UK

Basel, Switzerland
On-site (minimum of three days per week)
Parenteral drug development
Peptide formulation
Manufacturing process development
Roche UK is seeking an Expert in Drug Product Formulation and Processing for Synthetic Molecule Parenterals to join their Pharmaceutical Development team in Basel, Switzerland. The role requires extensive expertise in peptide formulation and drug development processes, along with strong collaboration and mentoring skills

Job Summary

  • The Pharmaceutical Development DP SM Parenterals group is responsible for the development of parenteral drug products Synthetic molecules from Phase 1 through Launch.
  • The position requires deep scientific expertise and strategic vision to support the drug development portfolio (CMC expertise) and drive innovation within cross-functional teams.
  • We are looking for candidates based in or willing to relocate to Basel, with the expectation of working from the office a minimum of three days per week.

Matching Summary

Match Score: 85

Roche UK is seeking an Expert in Drug Product Formulation and Processing for Synthetic Molecule Parenterals to join their Pharmaceutical Development team in Basel, Switzerland. The role requires extensive expertise in peptide formulation and drug development processes, along with strong collaboration and mentoring skills.

Skills & Requirements

Must-have

  • parenteral drug development
  • peptide formulation
  • manufacturing process development
  • regulatory CMC documents
  • cross-functional collaboration

Nice-to-have

  • strategic vision
  • cutting-edge practices
  • problem-solving mindset
  • passion for innovation

Key Requirements

  • Ph.D. or master’s degree
  • minimum of 6 years of industry experience
  • authoring Drug Product (DP) sections of an NDA
  • developing and launching peptide combination products
  • peptide analytical techniques
  • aseptic manufacturing processes
  • scale-up
  • technology transfers
  • regulatory and quality requirements
  • writing and reviewing regulatory CMC source and submission documents

Work Rights

Not specified

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